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Research 661–690 of 1000+
- MmuPV1-Induced Cutaneous Squamous Cell Carcinoma Arises Preferentially from Lgr5+ Epithelial Progenitor Cells
- Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin
- Integration of Point-of-Care Technology in the Decoding Process of Single Nucleotide Polymorphism for Healthcare Application †
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion
- Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Clinical and Genetic Aspects of Alopecia Areata: A Cutting Edge Review
- Genetic association of wool quality characteristics in United States Rambouillet sheep
- Hormonal and Genetic Etiology of Male Androgenetic Alopecia
- FLCN regulates transferrin receptor 1 transport and iron homeostasis
- Current Genetics in Hair Diseases
- LHX2: a transcription factor in development, homeostasis, repair, and disease
- Transcriptomic crossroads: Decoding genes and pathways that connect alopecia areata with chronic inflammatory skin disorders
- Genetic Variation in CYP2B6, UGT1A4 and Sulfotransferases Is Associated with Disease-Free Survival in South African Breast Cancer Patients Treated with Tamoxifen
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Role of MEG3-miRNAs in immune-inflammatory regulation in age-dependent wool follicle remodeling in Tan sheep
- JAK-Inhibitors Beyond the Label: Emerging Applications in Dermatology
- Predicting Physical Appearance from Low Template: State of the Art and Future Perspectives
- Association of JAK 1 and JAK 2 gene polymorphism with alopecia areata risk: a case–control genetic study
- Keratin 15 promotes a progenitor cell state in basal keratinocytes of skin epidermis
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts
- The Genetics of Acne
- Genetic architecture of thermotolerance traits in beef cattle: a novel integration of SNP and breed-of-origin effects
- Alopecia Areata: Understanding the Pathophysiology and Advancements in Treatment Modalities
- Evolution of long scalp hair in humans
- Signal integrator function of CXXC5 in Cancer
- Biomedical applications of organoids in genetic diseases
- Pathogenesis and management of TRPV3-related Olmsted syndrome